Standard

2-Hydroxy-3-octyloxybenzaldehyde. / Novoselova, Julia V.; Vereshchagin, Anatoliy A.; Kalnin, Arseniy Y.; Lukyanov, Daniil A.; Levin, Oleg V.

в: MolBank, Том 2021, № 3, M1264, 03.08.2021.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Novoselova, JV, Vereshchagin, AA, Kalnin, AY, Lukyanov, DA & Levin, OV 2021, '2-Hydroxy-3-octyloxybenzaldehyde', MolBank, Том. 2021, № 3, M1264. https://doi.org/10.3390/M1264

APA

Novoselova, J. V., Vereshchagin, A. A., Kalnin, A. Y., Lukyanov, D. A., & Levin, O. V. (2021). 2-Hydroxy-3-octyloxybenzaldehyde. MolBank, 2021(3), [M1264]. https://doi.org/10.3390/M1264

Vancouver

Novoselova JV, Vereshchagin AA, Kalnin AY, Lukyanov DA, Levin OV. 2-Hydroxy-3-octyloxybenzaldehyde. MolBank. 2021 Авг. 3;2021(3). M1264. https://doi.org/10.3390/M1264

Author

Novoselova, Julia V. ; Vereshchagin, Anatoliy A. ; Kalnin, Arseniy Y. ; Lukyanov, Daniil A. ; Levin, Oleg V. / 2-Hydroxy-3-octyloxybenzaldehyde. в: MolBank. 2021 ; Том 2021, № 3.

BibTeX

@article{828c73aaf33e4b9d9bb3113ba4c250b0,
title = "2-Hydroxy-3-octyloxybenzaldehyde",
abstract = "Herein, we report the chromatography-free synthesis of 2-hydroxy-3-octyloxybenzaldehyde by the alkylation of 2,3-dihydroxybenzaldehyde as a promising precursor for new SalEn-type complexes with transition metals. The structure of the product is elucidated by means of 1H and 13C-NMR spectra, high-resolution mass spectrometry with electrospray ionization (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).",
keywords = "2-hydroxy-3-octylbenzaldehyde, Alkylation, SalEn precursor, Schiff base, DESIGN, COMPLEXES, NI-SALEN, OXYGEN, NICKEL, REDUCTION, alkylation, ELECTROCHEMICAL SENSOR, CATALYSTS",
author = "Novoselova, {Julia V.} and Vereshchagin, {Anatoliy A.} and Kalnin, {Arseniy Y.} and Lukyanov, {Daniil A.} and Levin, {Oleg V.}",
note = "Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2021",
month = aug,
day = "3",
doi = "10.3390/M1264",
language = "English",
volume = "2021",
journal = "MolBank",
issn = "1422-8599",
publisher = "MDPI AG",
number = "3",

}

RIS

TY - JOUR

T1 - 2-Hydroxy-3-octyloxybenzaldehyde

AU - Novoselova, Julia V.

AU - Vereshchagin, Anatoliy A.

AU - Kalnin, Arseniy Y.

AU - Lukyanov, Daniil A.

AU - Levin, Oleg V.

N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

PY - 2021/8/3

Y1 - 2021/8/3

N2 - Herein, we report the chromatography-free synthesis of 2-hydroxy-3-octyloxybenzaldehyde by the alkylation of 2,3-dihydroxybenzaldehyde as a promising precursor for new SalEn-type complexes with transition metals. The structure of the product is elucidated by means of 1H and 13C-NMR spectra, high-resolution mass spectrometry with electrospray ionization (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).

AB - Herein, we report the chromatography-free synthesis of 2-hydroxy-3-octyloxybenzaldehyde by the alkylation of 2,3-dihydroxybenzaldehyde as a promising precursor for new SalEn-type complexes with transition metals. The structure of the product is elucidated by means of 1H and 13C-NMR spectra, high-resolution mass spectrometry with electrospray ionization (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).

KW - 2-hydroxy-3-octylbenzaldehyde

KW - Alkylation

KW - SalEn precursor

KW - Schiff base

KW - DESIGN

KW - COMPLEXES

KW - NI-SALEN

KW - OXYGEN

KW - NICKEL

KW - REDUCTION

KW - alkylation

KW - ELECTROCHEMICAL SENSOR

KW - CATALYSTS

UR - http://www.scopus.com/inward/record.url?scp=85112280880&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/9a697ae1-7cb8-379d-8897-32eb8969060e/

U2 - 10.3390/M1264

DO - 10.3390/M1264

M3 - Article

AN - SCOPUS:85112280880

VL - 2021

JO - MolBank

JF - MolBank

SN - 1422-8599

IS - 3

M1 - M1264

ER -

ID: 84798169